EP1605069B1 - Bleifreies Lager für Kraftstoffeinspritzpumpe - Google Patents
Bleifreies Lager für Kraftstoffeinspritzpumpe Download PDFInfo
- Publication number
- EP1605069B1 EP1605069B1 EP05012357A EP05012357A EP1605069B1 EP 1605069 B1 EP1605069 B1 EP 1605069B1 EP 05012357 A EP05012357 A EP 05012357A EP 05012357 A EP05012357 A EP 05012357A EP 1605069 B1 EP1605069 B1 EP 1605069B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- phase
- hard particles
- mass
- alloy
- hard
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Not-in-force
Links
- 238000002347 injection Methods 0.000 title claims description 22
- 239000007924 injection Substances 0.000 title claims description 22
- 239000002245 particle Substances 0.000 claims description 100
- 239000000446 fuel Substances 0.000 claims description 33
- 239000011159 matrix material Substances 0.000 claims description 13
- 239000012535 impurity Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000012071 phase Substances 0.000 description 58
- 229910000881 Cu alloy Inorganic materials 0.000 description 32
- 229910045601 alloy Inorganic materials 0.000 description 29
- 239000000956 alloy Substances 0.000 description 29
- 238000005245 sintering Methods 0.000 description 23
- 239000010949 copper Substances 0.000 description 22
- 239000000463 material Substances 0.000 description 19
- 229910052797 bismuth Inorganic materials 0.000 description 15
- 239000000843 powder Substances 0.000 description 14
- 229910052745 lead Inorganic materials 0.000 description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 9
- 229910000765 intermetallic Inorganic materials 0.000 description 8
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 229910001152 Bi alloy Inorganic materials 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 238000005461 lubrication Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229910000906 Bronze Inorganic materials 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 2
- 239000010974 bronze Substances 0.000 description 2
- 230000008094 contradictory effect Effects 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000009766 low-temperature sintering Methods 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910003178 Mo2C Inorganic materials 0.000 description 1
- 229910018605 Ni—Zn Inorganic materials 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- 229910020220 Pb—Sn Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 229910052961 molybdenite Inorganic materials 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 238000010587 phase diagram Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
- C22C32/0047—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
- C22C32/0073—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only borides
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
- C22C32/0089—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with other, not previously mentioned inorganic compounds as the main non-metallic constituent, e.g. sulfides, glass
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C33/00—Parts of bearings; Special methods for making bearings or parts thereof
- F16C33/02—Parts of sliding-contact bearings
- F16C33/04—Brasses; Bushes; Linings
- F16C33/06—Sliding surface mainly made of metal
- F16C33/12—Structural composition; Use of special materials or surface treatments, e.g. for rust-proofing
- F16C33/121—Use of special materials
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C33/00—Parts of bearings; Special methods for making bearings or parts thereof
- F16C33/02—Parts of sliding-contact bearings
- F16C33/04—Brasses; Bushes; Linings
- F16C33/06—Sliding surface mainly made of metal
- F16C33/14—Special methods of manufacture; Running-in
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C2204/00—Metallic materials; Alloys
- F16C2204/10—Alloys based on copper
- F16C2204/18—Alloys based on copper with bismuth as the next major constituent
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C2220/00—Shaping
- F16C2220/20—Shaping by sintering pulverised material, e.g. powder metallurgy
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C2220/00—Shaping
- F16C2220/40—Shaping by deformation without removing material
- F16C2220/44—Shaping by deformation without removing material by rolling
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C2220/00—Shaping
- F16C2220/80—Shaping by separating parts, e.g. by severing, cracking
- F16C2220/82—Shaping by separating parts, e.g. by severing, cracking by cutting
Definitions
- the present invention relates to a bearing used for a fuel-injection pump, more particularly, a copper-based sintered alloy bearing free of Pb, having improved sliding properties.
- a fuel injector of a diesel engine finely pulverizes the fuel and uniformly mixes it with air in sprayed state, and imparts to the fuel-air mixture the requisite pressure for injection.
- the fuel injector plays the role of injecting fuel into a combustion engine in appropriate injection amount and at appropriate injection time, which amount and time are dependent upon the load and rotation of the engine.
- a fuel injection pump is usually driven by a crankshaft of an engine with the aid of a belt. Since the fuel injection pump is a cantilever construction, the belt tension imparts to the fuel injection pump a local load. Although the fuel of the engine lubricates the bearing, the sliding condition of the bearing is liable to be the boundary-lubricating condition because of the low viscosity of fuel and the local load. Material of the bearing should, therefore, be highly wear-resistant and seizure-resistant. Recently, attempts have been made to decrease the sulfur content of light-oil fuel used in a Diesel engine in the light of environmental protection. The lubrication property of the fuel decreases accordingly, and, therefore, the wear resistance becomes particularly important.
- lead bronze has been frequently used for the bearing of a fuel injection pump. Its composition is for example 3.0% of Sn, 23.0% of Pb, 3.0% of Fe, 1.0% of P and the balance of Cu. Fe among these components precipitates as hard particles and contributes to enhance the wear resistance.
- pressure of the fuel injector should be high.
- the pressure is dependent upon the revolution speed of the engine, high pressure is difficult to obtain at low revolution and high load of the engine.
- NOx is formed in great amount and noise is seriously incurred.
- such parts of the fuel injection pump are shown: 1 - eccentric cam, 2 - bearing (bushing), 3 - housing of a ring cam, 4 - housing, 5 - highpressure valve, 6 - plunger, 7 - suction-control valve, 8 - feeding pump, 9 - cam shaft, 10 - suction valve, and 11 - connecting pipe.
- the bearing is subjected to reciprocating pressure of the fuel and its pressure on the surface of the bearing 2 is very high due to the pressure-increasing tendency as described hereinabove.
- the thickness of the oil film on the bearing is extremely thin. Since the bearing is used under such conditions, high level of wear resistance and seizure resistance are required in the bearing.
- a lead-containing bearing or a resin bearing is used at present for the bearing of a fuel injection pump.
- the bushing used in the fuel injection pump is exposed to more severe boundary-lubrication condition as compared with the general bushing.
- the wear resistance, seizure resistance, corrosion-resistance and the like required for the former bushing is at higher level than those of the latter. Therefore, lead bronze has been used for the bushing of a fuel injection pump.
- Lead (Pb) added to the copper alloy for the sliding material expands and is deforms in the sliding direction on the sliding surface, upon temperature rise during the sliding. Lead (Pb), therefore, cools the sliding surface, and prevents seizure due to its excellent self lubricating property. Since lead (Pb) forms a soft dispersion phase in the copper alloy, lead has compatibility and foreign matters are embedded in the lead phase.
- Japanese Examined Patent Publication (kokoku) No. 8-19945 proposes dispersion of fine lead particles expressed in a particular calculating formula.
- the total lead (Pb) particles are observed in the field of 0.1mm 2 (10 5 ⁇ m 2 ), i.e. S t , to obtain their number (N) and area (S p ) in ⁇ m 2 .
- the proposed formula of S p /S t /N is construed to be ratio of 0.1% or less.
- Japanese Unexamined Patent Publication (kokoku) No. 10-330868 (hereinafter referred to as "the patent document 3") proposes a Pb-free alloy which attains the sliding properties as high as that of the sintered Cu-Pb alloy.
- the patent document 3 proposes a Pb-free alloy which attains the sliding properties as high as that of the sintered Cu-Pb alloy.
- a drawing of this publication shows that Bi is present on the grain-boundary triple points and the grain boundaries in the vicinity of the triple points.
- Japanese Patent No. 3,421,724 proposes the following sintered copper alloy. That is, the hard particles are present in and mixed with the Pb or Bi phase. This phase is not separated from sintered alloy, even if Pb and Bi become flowable upon temperature rise.
- the Pb and Bi phase behaves as a cushion of the hard particles, so that when the hard particles and the opposite shaft are brought into sliding contact with one another, the hard particles are forced into the Pb or Bi phase.
- the aggressive properties of the hard particles are, therefore, mitigated.
- the hard particles are separated from the Pb or Bi phase, they are again captured by the Pb or Bi phase. The abrasive wear due to the separated hard particles is, therefore, mitigated. Since the hard particles are enveloped in the Bi phase, the size of the Bi phase is greater than that of the hard particles.
- Japanese Unexamined Patent Publication (kokai) No. 2001-220630 proposes the following Cu-Bi(Pb) based sintered alloy, particularly a structure of the alloy, wherein the intermetallic-compound particles are present around the Bi or Pb phase.
- the Bi or Pb phase and Cu alloy primarily wear out, while the intermetallic compound particles remain on the surface and protrude on the surface of sintered alloy.
- the concave Bi or Pb phase and Cu alloy act as oil reserving portions. As a result, the wear resistance and fatigue resistance are improved.
- An example of the sintering conditions is 800-920°C for approximately 15 minutes.
- Pb and Bi contained in the Cu alloy forms a separate phase from the Cu matrix, because Pb and Bi are virtually not dissolved in the solid Cu, and they do not form intermetallic compounds.
- Such structure and properties of Pb and Bi are utilized in the conventional copper alloys as a compatibile property. Meanwhile, Pb and Bi are of low strength, and the fatigue strength is lowered. Therefore, the low-temperature sintering and formation of the fine Pb phase proposed in the patent document 1 is effective for mitigating the drawbacks mentioned above. However, the low temperature at sintering detrimentally lowers the bonding strength of the copper alloy particles.
- the Bi phase of the Cu-Bi based alloys proposed by the patent documents 3, 4 and 5 exudes on the surface of the alloys or corrodes, when the alloys are used at high temperature or in deteriorated oil.
- the amount of Bi of the Cu-Bi based alloys used becomes less than the added amount, with the result that the sliding properties are impaired.
- Bismuth (Bi) may also be dissolved in the lubricating oil.
- the Bi phase is finely dispersed, the volume of each Bi particle is so small that the exudation and decrease in the Bi content can be prevented.
- the fine dispersion of Bi and high post-sintering strength of copper alloys are contradictory phenomena.
- the Bi phase of the Bi-containing Cu alloys of the patent documents 4 and 5 is converted to liquid during sintering.
- the components of the Cu matrix are, therefore, liable to diffuse into the liquid Bi phase.
- Intermetallic compounds are, therefore, formed in the liquid phase. Since the resultant intermetallic compounds are always present in the boundary of the Bi phase and Cu matrix, the intermetallic compounds outside the Cu phase cannot be held by the Cu phase.
- the sintering is carried out for a long period of time.
- the size of the Bi phase becomes greater than the size of the hard particles.
- Figure 2 of the patent document 4 suggests such growth of the Bi phase. It appears that the hard-particle contact ratio described hereinafter is almost 100% in the patent document 4. As shown in Fig. 1 of the patent document No. 5, the hard-particle contact proportion is high in this patent document.
- the Bi phase of the prior art is one of the reasons for the lowering the fatigue resistance and the corrosion resistance.
- a lead-free bearing which contains from 1 to 30 mass % of Bi and from 0.1 to 10 mass % of hard particles having from 10 to 50 ⁇ m of the average particle diameter, the balance being Cu and unavoidable impurities, and further the Bi phase dispersed in the Cu matrix has average particle diameter smaller than that of the hard particles.
- a lead-free bearing which contains from 1 to 30 mass % of Bi and from 0.1 to 10 mass % of hard particles having from 10 to 50 ⁇ m of average particle diameter, the balance being Cu and unavoidable impurities, and which includes a Bi phase in contact with a portion of the hard particles, the contact length of which with the Bi phase being 50% or less relative to the total circumference length of the Bi phase, the number of said portion of the hard particles being 70% or more of the total hard particles.
- the Bi content is from 1 to 30 mass %, because the seizure resistance is poor at Bi content less than 1 mass %, and, further, the strength is low and the fatigue resistance is poor at Bi content more than 30 mass %.
- Preferred Bi content is from 1 to 15 mass %.
- the hard particles herein may be those proposed in the patent document 2.
- An Fe-based compound having excellent sintering property with the copper alloy such as Fe 2 P, Fe 3 P, FeB, Fe 2 B, and Fe 3 B, is preferably used.
- the Fe-based compound has poor wettability with the bismuth (Bi) and good wettability with copper (Cu)
- the contact proportion between the Bi phase and the hard particles is low after sintering.
- the hard particles are likely to be held by the Cu matrix. The separation of the hard particles and crack formation in the hard particles, which results in deterioration of the wear resistance and seizure resistance, are, therefore, difficult to occur during sliding.
- the content of the hard particles is less than 0.1 mass %, the seizure resistance and the wear resistance are poor. On the other hand, when the content of the hard particles is more than 10 mass %, the strength and the fatigue resistance are lowered. In addition, the opposite material is liable to be attacked by the hard particles, and the sintering property is also impaired.
- Preferred content of the hard particles is from 1 to 5 mass %.
- the balance of the above components is Cu and unavoidable impurities.
- the impurities, including Pb are ordinary ones.
- an additive element(s) may be added to the copper alloy.
- phosphorus (P) which lowers the melting point of the copper alloy and improves the sintering properties, may be added up to 0.5 mass %.
- Tin (Sn) which enhances the strength and fatigue resistance, may be added within a range of from 1 to 15 mass %.
- Sn content is less than 1 mass %, the strength is not enhanced satisfactorily.
- intermetallic compounds are liable to form and the alloy embritles.
- Nickel (Ni) which enhances the strength and the corrosion resistance, may be added within a range of from 0.1 to 5 mass %. When the nickel (Ni) content is less than 0.1 mass %, the strength does not increase satisfactorily. On the other hand, when the nickel (Ni) content is more than 5 mass %, intermetallic compounds are liable to form and the alloy embritles. These elements are alloyed in Cu and are constitutional elements of the copper-alloy matrix.
- a solid lubricant such as MoS 2 and graphite may be added to the copper alloy.
- the solid lubricant is not alloyed with the copper alloy but is present in the copper alloy as a composite component.
- the solid lubricant may be added up to 5 mass %.
- the average diameter of the hard particles is from 10 to 50 ⁇ m.
- the average particle diameter is less than 10 ⁇ m, the hard particles are not effective to improve the wear resistance.
- the particle diameter is more than 50 ⁇ m, the strength of the sintered copper alloy is low.
- Preferred average diameter of the hard particles is from 15 to 30 ⁇ m.
- the alloy structure according to the present invention is such that the flow of the Bi phase is suppressed as much as possible and hence the contact between the Bi phase and hard particles due to flow of the Bi phase is suppressed.
- This feature is defined in the first bearing according to the present invention as D Bi ⁇ D H .
- D Bi indicates average particle-diameter of the Bi phase, i.e., the diameter of a circle of a Bi phase.
- D H indicates the average particle diameter of the hard particles.
- the second bearing according to the present invention includes a Bi phase in contact with a portion of the hard particles, the contact length of which with the Bi phase being 50% or less relative to the total circumference length of the Bi phase, the number of said portion of the hard particles being 70% or more of the total hard particles.
- the "contact length of a portion of the hard particles with the Bi phase relative to the total circumference length of the Bi phase” is hereinafter referred to as "the hard-particle contact ratio" .
- the descriptions of the hard particles in the present paragraph relate to those in contact with the Bi phase, unless otherwise specified.
- the hard-particle contact ratio is 100%, the entire circumference of one or more hard particles is in contact with the Bi phase. This contact state is realized with each of the hard particles. This state is nothing but that the hard particles are embedded or enclosed in the Bi phase.
- the hard-particle contact ratio is less than 100% but more than 0%, the hard particles in contact with the Bi phase have necessarily a portion protruding outside the Bi phase. This portion is in contact with the copper alloy.
- the hard-particle contact ratio is 50% or less, because the contact between the hard particles and the matrix is decreased to be as small as possible. In this state, the respective properties of the hard particles and the copper matrix can be exhibited at high level.
- the proportion of number of the hard particles having 50% or less of the hard particle contact ratio relative to the total hard particles, which may include those not in contact with the Bi phase, is referred to as the "hard particle ratio".
- the hard particle ratio is 100%, all of the hard particles have 50% or less of the hard particle contact ratio.
- the hard particle ratio is 0%, all of the hard particles have more than 50% of the hard particle contact ratio.
- the hard particle ratio is limited to 70% or more, because the Bi phase and hard particles, which are slightly in contact with one another, should be present in the alloy in a relatively large proportion. As a result, the respective properties of the Bi phase and the hard particles are exhibited satisfactorily.
- the sintering temperature of Cu-Bi alloy atomized powder or Cu-Bi alloy mixture powder is held at sintering temperature for a short time of 2 minutes or shorter.
- Such sintering can be carried out by the high-frequency induction sintering proposed by one of the present applicants in Japanese Unexamined Patent Publication (kokai) 2002-12902 (patent document 6).
- the Bi phase of the copper-based sintered alloy according to the present invention exhibits compatibility.
- the hard particles are firmly held by the matrix of the copper-based sintered alloy according to the present invention and are not easily separated from the Cu matrix.
- the wear resistance and the seizure resistance are, therefore, improved.
- the strength and the fatigue resistance are improved.
- the Cu-Bi alloy is pulverized by an atomizing method.
- the resultant Cu-Bi powder is mixed with hard-particle powder and powder of the other metallic components.
- the components other than the hard-particle powder may be in the form of an alloy powder prepared by the atomizing method.
- the powder mixture is dispersed on a steel sheet to a uniform thickness and is subjected to the sintering for a short period of time described hereinafter.
- the sintered alloy layer is rolled, then followed by sintering for a short period of time. If necessary, the rolling is carried out again.
- the resultant sintered and rolled product is in the form of a bimetal, which is cut into a pre-determined shape.
- the cut sheet is bent into cylindrical form and is worked into a bushing.
- the Cu-Bi alloy powder the composition of which is shown in Table 1 (the atomized powder, 150 ⁇ m or less of the average particle diameter) and the hard-particle powder (the average particle diameter is shown in Table 1) were mixed and sprayed on a steel sheet to a thickness of approximately 1 mm.
- the primary sintering was carried out at 750 ⁇ 1000C for 20 ⁇ 1800 seconds in the hydrogen reducing gas.
- the rolling was subsequently carried out.
- the secondary sintering was carried out under the same conditions as the primary sintering.
- the resultant sintered materials were used as the test materials.
- the sintering for a long period of time within the range of the above mentioned sintering time promotes the diffusion of the Bi phase and hence to prepare comparative samples..
- the surface of the copper alloys prepared by the above mentioned method was lapped by abrasive paper to adjust the surface roughness (ten-point average roughness) to 1.0 ⁇ m or less.
- a steel ball was abutted on the so-prepared surface and was caused to slide into one direction under load. The surface of the steel ball was then observed to measure the surface area of Cu alloy adhered on the steel ball. Since the easily adhered material has poor seizure resistance, the small adhesion area indicates improved seizure resistance.
- the fatigue strength and tensile strength show good co-relationship with one another. Improved fatigue strength is, therefore, attained at high tensile strength.
- the tensile strength test stipulated in JIS was carried out to measure the tensile strength of the Cu-Bi alloys and was used as an alternative property.
- the inventive examples exhibit high level of improved seizure resistance, fatigue resistance and corrosion resistance.
- FIGs. 1 and 2 Microscopic photograph of the inventive example No. 4 is shown in Figs. 1 and 2, at magnification of 200 and 500, respectively.
- Microscopic photograph of the comparative example No. 3 is shown in Figs. 3 and 4, at magnification of 200 and 500, respectively.
- the contact between the hard particles and the Bi phase is in lower proportion than that in the latter photographs of Figs. 3 and 4.
- the circle of a Bi phase indicates a circle which surrounds a Bi phase, appearing like one irregularly shaped particle, and which is in contact with the largest periphery of such Bi phase.
- Comparative material No. 4 and inventive material No. 6 shown in Table 1 were bent into a cylindrical form and worked as a bushing. This was mounted in a fuel injection pump of a diesel engine and a durability test was carried out using light oil corresponding to JIS second class as the lubricating oil. No damage or failure occurred with the case of the inventive material No.6 during the test period of 1,000 hours.
- the bearing of a fuel injection pump according to the present invention is free of Pb but exhibits improved seizure resistance and fatigue resistance.
- the bearing is therefore appropriate to be operated in a pump under high pressure
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Powder Metallurgy (AREA)
- Sliding-Contact Bearings (AREA)
Claims (4)
- Bleifreies Lager für eine Kraftstoffeinspritzpumpe, das 1 bis 30 Masse-% Bi, gegebenenfalls mindestens ein Element, ausgewählt aus der Gruppe, bestehend aus 1 bis 15 Masse-% Sn, 0,1 bis 5 Masse-% Ni und nicht mehr als 0,5 Masse-% P, und 0,1 bis 10 Masse-% harter Partikel mit einem durchschnittlichen Partikeldurchmesser von 10 bis 50 µm enthält, wobei der Rest Cu und unvermeidbare Verunreinigungen darstellt, dadurch gekennzeichnet, dass die in der Cu-Matrix dispergierte Bi-Phase einen kleineren durchschnittlichen Partikeldurchmesser aufweist als derjenige der harten Partikel.
- Bleifreies Lager für eine Kraftstoffeinspritzpumpe, das 1 bis 30 Masse-% Bi und 0,1 bis 10 Masse-% harter Partikel mit einem durchschnittlichen Partikeldurchmesser von 10 bis 50 µm enthält, wobei der Rest Cu und unvermeidbare Verunreinigungen darstellt, unddaseine Bi-Phase enthält, die in Kontakt mit einem Teil der harten Partikel steht, wobei die Kontaktlänge hiervon mit der Bi-Phase 50% oder weniger, relativ zur gesamten Umfangslänge der Bi-Phase, und die Anzahl des Teils der harten Partikel 70% oder mehr der gesamten harten Partikel beträgt.
- Bleifreies Lager nach Anspruch 1 oder 2, wobei es weiterhin mindestens ein Element, ausgewählt aus der Gruppe, bestehend aus 1 bis 15 Masse-% Sn, 0,1 bis 5 Masse-% Ni und nicht mehr als 0,5 Masse-% P enthält.
- Bleifreies Lager nach irgendeinem der Ansprüche 1 bis 3, worin die harten Partikel aus einer Eisenverbindung bestehen, ausgewählt aus Fe2P, Fe3P, FeB, Fe2B und Fe3B.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004172349A JP4410612B2 (ja) | 2004-06-10 | 2004-06-10 | 燃料噴射ポンプ用Pbフリー軸受 |
JP2004172349 | 2004-06-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1605069A1 EP1605069A1 (de) | 2005-12-14 |
EP1605069B1 true EP1605069B1 (de) | 2007-08-15 |
Family
ID=34937322
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05012357A Not-in-force EP1605069B1 (de) | 2004-06-10 | 2005-06-08 | Bleifreies Lager für Kraftstoffeinspritzpumpe |
Country Status (5)
Country | Link |
---|---|
US (1) | US7883588B2 (de) |
EP (1) | EP1605069B1 (de) |
JP (1) | JP4410612B2 (de) |
CN (1) | CN100383270C (de) |
DE (1) | DE602005001976T2 (de) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT413034B (de) * | 2003-10-08 | 2005-10-15 | Miba Gleitlager Gmbh | Legierung, insbesondere für eine gleitschicht |
JP4476634B2 (ja) | 2004-01-15 | 2010-06-09 | 大豊工業株式会社 | Pbフリー銅合金摺動材料 |
JP4410612B2 (ja) | 2004-06-10 | 2010-02-03 | 大豊工業株式会社 | 燃料噴射ポンプ用Pbフリー軸受 |
EP2048253B1 (de) * | 2006-08-05 | 2019-05-01 | Taiho Kogyo Co., Ltd | Verfahren zur herstellung eines gleitwerkstoffes aus gesinterter blei-freier kupferlegierung |
US8679641B2 (en) * | 2007-01-05 | 2014-03-25 | David M. Saxton | Wear resistant lead free alloy bushing and method of making |
US20120114971A1 (en) * | 2007-01-05 | 2012-05-10 | Gerd Andler | Wear resistant lead free alloy sliding element method of making |
JP5289065B2 (ja) * | 2007-02-14 | 2013-09-11 | 大豊工業株式会社 | Pbフリー銅基焼結摺動材料 |
CN101688268B (zh) | 2007-05-15 | 2012-07-11 | 大丰工业株式会社 | 不含Pb的铜合金滑动材料和滑动轴承 |
JP2009083009A (ja) * | 2007-09-28 | 2009-04-23 | Aisin Aw Co Ltd | 切削工具 |
US20090202855A1 (en) * | 2008-01-09 | 2009-08-13 | Saxton David M | Porous sliding bearing and method of construction thereof |
JP5386373B2 (ja) | 2008-01-23 | 2014-01-15 | 大豊工業株式会社 | 焼結銅合金摺動材の製造方法及び焼結銅合金摺動材 |
JP5328256B2 (ja) * | 2008-08-04 | 2013-10-30 | キヤノン株式会社 | 吸入装置 |
KR101696562B1 (ko) | 2008-09-10 | 2017-01-13 | 다이호 고교 가부시키가이샤 | Pb 프리 Cu-Bi계 소결 재료제 슬라이딩 부품 |
CA2793587C (en) | 2009-03-19 | 2016-01-19 | Daniel Young | Pouch for internal mixture of segregated reactants and applications thereof |
US8211250B1 (en) | 2011-08-26 | 2012-07-03 | Brasscraft Manufacturing Company | Method of processing a bismuth brass article |
US8465003B2 (en) | 2011-08-26 | 2013-06-18 | Brasscraft Manufacturing Company | Plumbing fixture made of bismuth brass alloy |
JP5340355B2 (ja) | 2011-08-30 | 2013-11-13 | 大同メタル工業株式会社 | 銅系摺動材料 |
CN102689013A (zh) * | 2012-06-06 | 2012-09-26 | 海安县鹰球集团有限公司 | 铁基粉末冶金高韧性含油轴承及其制造方法 |
JP5636033B2 (ja) * | 2012-12-28 | 2014-12-03 | 大同メタル工業株式会社 | 摺動部材及びこれを用いた軸受装置 |
JP6363931B2 (ja) * | 2014-10-14 | 2018-07-25 | 大豊工業株式会社 | すべり軸受用銅合金 |
US10125818B2 (en) * | 2014-12-19 | 2018-11-13 | Cummins Ltd. | Turbomachine shaft and journal bearing assembly |
JP6752671B2 (ja) * | 2016-09-30 | 2020-09-09 | 大同メタル工業株式会社 | 摺動材料およびその製造方法並びに摺動部材 |
CN106544541B (zh) * | 2016-11-14 | 2018-01-26 | 合肥工业大学 | 一种高强无铅铜基滑动材料及其制备方法 |
CN110406201B (zh) * | 2019-08-21 | 2020-09-25 | 大连理工大学 | 一种自润滑双金属层状复合材料及其制备方法和应用 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH079046B2 (ja) | 1984-07-07 | 1995-02-01 | トヨタ自動車株式会社 | 銅系焼結体 |
JPS6173849A (ja) | 1984-09-19 | 1986-04-16 | Takeshi Masumoto | Cu基超伝導合金 |
JP3298634B2 (ja) * | 1990-02-27 | 2002-07-02 | 大豊工業株式会社 | 摺動材料 |
JP2918292B2 (ja) * | 1990-05-25 | 1999-07-12 | 大豊工業株式会社 | 摺動材料 |
JPH0819945B2 (ja) | 1992-02-28 | 1996-03-04 | 大同メタル工業株式会社 | 高荷重用多層鉛青銅軸受 |
JP3501288B2 (ja) * | 1995-03-03 | 2004-03-02 | 大豊工業株式会社 | 摺動材料及びその表面処理方法 |
JP3339780B2 (ja) * | 1996-07-30 | 2002-10-28 | エヌデーシー株式会社 | 耐摩耗性に優れる摺動材料 |
JPH10330868A (ja) * | 1997-06-04 | 1998-12-15 | Toyota Motor Corp | 銅基焼結合金 |
JP4188440B2 (ja) * | 1997-10-17 | 2008-11-26 | 大豊工業株式会社 | 摺動特性及び被削性に優れた銅系焼結摺動材料 |
JP3421724B2 (ja) * | 1999-09-13 | 2003-06-30 | 大同メタル工業株式会社 | 銅系摺動材料 |
JP2001107106A (ja) * | 1999-10-12 | 2001-04-17 | Ndc Co Ltd | 銅系焼結摺動材料 |
JP3932159B2 (ja) | 2000-02-02 | 2007-06-20 | 大豊工業株式会社 | バイメタル状軸受合金の高周波焼結方法 |
JP3507388B2 (ja) | 2000-02-08 | 2004-03-15 | 大同メタル工業株式会社 | 銅系摺動材料 |
JP2001240925A (ja) * | 2000-02-29 | 2001-09-04 | Daido Metal Co Ltd | 銅系摺動材料 |
DE10045604A1 (de) * | 2000-09-15 | 2002-03-28 | Mitsubishi Polyester Film Gmbh | Mehrschichtige biaxial orientierte Polyesterfolie mit optimierter elektrischer Leitfähigkeit über die Dicke |
JP2003194061A (ja) * | 2001-12-27 | 2003-07-09 | Daido Metal Co Ltd | 銅系焼結摺動材料およびその製造方法 |
JP4476634B2 (ja) * | 2004-01-15 | 2010-06-09 | 大豊工業株式会社 | Pbフリー銅合金摺動材料 |
JP4410612B2 (ja) | 2004-06-10 | 2010-02-03 | 大豊工業株式会社 | 燃料噴射ポンプ用Pbフリー軸受 |
-
2004
- 2004-06-10 JP JP2004172349A patent/JP4410612B2/ja not_active Expired - Fee Related
-
2005
- 2005-06-08 EP EP05012357A patent/EP1605069B1/de not_active Not-in-force
- 2005-06-08 DE DE602005001976T patent/DE602005001976T2/de active Active
- 2005-06-09 US US11/148,186 patent/US7883588B2/en not_active Expired - Fee Related
- 2005-06-10 CN CNB2005100837977A patent/CN100383270C/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE602005001976T2 (de) | 2008-05-08 |
JP4410612B2 (ja) | 2010-02-03 |
JP2005350722A (ja) | 2005-12-22 |
CN100383270C (zh) | 2008-04-23 |
US20060000527A1 (en) | 2006-01-05 |
EP1605069A1 (de) | 2005-12-14 |
US7883588B2 (en) | 2011-02-08 |
DE602005001976D1 (de) | 2007-09-27 |
CN1721560A (zh) | 2006-01-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1605069B1 (de) | Bleifreies Lager für Kraftstoffeinspritzpumpe | |
EP2185303B1 (de) | Verschleissfeste buchse aus einer bleifreien legierung und herstellungsverfahren | |
EP1717325B1 (de) | Gleitmaterial aus pb-freier kupferlegierung | |
KR101242887B1 (ko) | 모터식 연료 펌프의 베어링 | |
EP1808503B1 (de) | Lager aus cu-sinterlegierung eines rezirkulationsabgasströmungsraten-regelventils oder dergleichen, eines egr-verbrennungsmotors mit hoher festigkeit und hervorragender abriebfestigkeit in hochtemperaturumgebung | |
JP3298634B2 (ja) | 摺動材料 | |
JP3839740B2 (ja) | 摺動材料 | |
US20010019779A1 (en) | Copper alloy sliding material | |
KR20090130128A (ko) | Pb 프리 구리 합금 슬라이딩 재료 및 미끄럼 베어링 | |
US5346668A (en) | Copper based alloy for wear resistant sliding layer and sliding member | |
GB2411211A (en) | Plain bearings for internal combustion engines | |
US5429876A (en) | Copper-lead based bearing alloy material excellent in corrosion resistance and a method of producing the same | |
US8715385B2 (en) | Bearing material |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20050610 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA HR LV MK YU |
|
AKX | Designation fees paid |
Designated state(s): DE FR GB |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE FR GB |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REF | Corresponds to: |
Ref document number: 602005001976 Country of ref document: DE Date of ref document: 20070927 Kind code of ref document: P |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20080516 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20150603 Year of fee payment: 11 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20150608 Year of fee payment: 11 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20160608 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20170228 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160630 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160608 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20220505 Year of fee payment: 18 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 602005001976 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20240103 |